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  • AAV Production Protocol
    Protocols 2025. 2. 15. 18:06

    1. Timeline

    - Day1: Cell seeding

    - Day2: Cell transfection

    - Day5: Cell harvest & lysis

     

     

    2. Protocol

     

    Day 1     Seed HEK293T cells with DMEM/10%FBS/1%a.a medium at each dish

    *  10cm dish: 4.0x106 cells

        15cm dish: 9.0x106 cells

    * Confluence at 70-80% next morning

     

    Day 2     Proceed transfection as below.

     

    * PEI solution (1ug/ul)

    - Dissolve ~100mg of branched PEI solution in ~10ml of DDW.

    - Dilute at 10ug/ul in DDW and adjust the pH to 7.0 with HCl.

    - Filter the solution through a 0.22um membrane, aliquot 0.5-1ml into sterile tubes, and store the tubes at -80℃

    * pAAV : pRepCap : pHelper = 1: 1: 2 (molar ratio)

    Plasmid Plasmid Size(bp) 100 mm dish 150 mm dish
    pAAV   6 ug 12 ug
    pRepCap   6 ug 12 ug
    pHelper   12 ug 24 ug
    Total bp   24 ug 48 ug

     

    - Prepare the plasmid/PEI mixture (1:3 ug ratio).

    1) For a 100 mm dish, add all three kinds of plasmid to tube 1 containing 0.5ml PBS, vortex and spin down.

    2) Add 72ul of PEI solution (1ug/ul) to tube 2 containing 0.5ml PBS, vortex and spin down.

    3) Transfer the solution from tube 1 to tube 2, vortex, spin down, and incubate for 5-10min at RT.

    4) Dropwise in the dish while mixing.

     

    Day 5     Harvest Virus.

     

    * Lysis Buffer

    Reagent                                                    Final Concentration

    1M Tris-HCl (pH 8.0)                                50 mM

    NaCl                                                         150 mM

    MgCl2                                                       2 mM

      - Sterilize using a disposable 0.45-µm filtration

      - hood and store at room temperature

     

    1) 72 hr after transfection, harvest cells and media with a scrapper.

    2) Transfer the cells and media into 50ml tubes.

    3) Centrifuge at 500 x g for 5 min to pellet the cells.

    4) Discard sup.

    5) Add 8.5 ml of Lysis buffer.

    6) Cell lysis

    - Freeze-thaw cell pellets 3 times at -80°C and 37°C to release the virus into the supernatant.

    - Vortex the cell pellets in between the freeze-thaw cycles

    7) Add 50U/ml Benzonase and Incubate in 37°C/ 30min

    8) Centrifuge at 4000 rpm for 10 min

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